Research Article

A Novel Missense WFS1 Variant: Expanding the Mutational Spectrum Associated with Nonsyndromic Low-Frequency Sensorineural Hearing Loss

Table 1

Summary of clinical data for members in the Chinese pedigree examined for genetic variants.

SubjectGenderAge at test (years)Age at onset (years)Use of aminoglycosidePTA (dB) right earPTA (dB) left earTinnitusVertigoLevel of hearing impairment

II-7F7030No6866NoNoSevere
III-6F5521No6060NoNoModerate
III-8M5813No5968NoNoSevere
III-10M6017No6468NoNoSevere
III-14F5516No7475NoNoSevere
III-16F539No7475NoNoSevere
III-20F4214No4441NoNoModerate
III-22M4414No4653NoNoModerate
IV-2F3011No3641NoNoModerate
IV-8M30No1313NoNoNormal
IV-10M3512No6058NoNoModerate
IV-12M307No7471NoNoSevere
IV-14F26No1114NoNoNormal
IV-22M3012No7166NoNoSevere
IV-29M168No3838NoNoModerate
V-1F63No4038NoNoModerate
V-3M131No8585NoNoProfound
V-8M10No2020NoNoNormal
V-9M4No1414NoNoNormal
V-15M55No2929NoNoMild